HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 54297241, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 54544880 | HCID 54544880 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 54297241 | HCID 54297241 | 70% |
Reaction Steps
A 15 mL round bottom flask was charged with (+)-(4aR)-(10bR)-8-(1-naphthyl)-10b-methyl-3,4,4a,5,6,10b-hexahydrobenzo[f]quinolin-3-one (22 mg, 0.065 mmol), 0.20 mL of t-butanol, and potassium t-butoxide (22 mg, 0.19 mmol). Methyl iodide (0.012 mL, 0.19 mmol) was added and the mixture was stirred at room temperature for 4 h. The mixture was diluted with ethyl acetate, and purified by silica gel chromatography (ethyl acetate eluent) to give 16 mg (70%) of the title compound as a yellow solid, upon trituration from diethyl ether/hexanes. mp 172°-173°. FDMS: m/e=353.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05670514 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-10bcbc5ef7c14ea0b102652c6dbfdba2 |
| Source note | uspto-grants-1997_09 |